Quality Electrodynamics recalls Siemens Knee and Extremity Coils with possible ferrous material in pushbutton assembly. Affected units have specific model numbers and serial ranges. Contact for return instructions.
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Quality Electrodynamics is recalling Siemens knee and extremity coils that may contain unintended ferrous material in the pushbutton assembly. This could pose a risk during MRI scans if the material causes interference or heating.
The pushbutton assembly in some coils may contain unintended ferrous material, which could cause heating or interference during MRI scans. This might lead to burns or other issues if the material interacts with the MRI's magnetic field.
Users of Siemens knee and extremity coils with model number 10185464 and serial numbers 1308-1311, 1313 are affected. Patients undergoing MRI scans with these coils are at risk of potential interference.
Check for Siemens model number 10185464 and serial numbers 1308, 1309, 1310, 1311, or 1313 on the coil's label. The product is sold under Quality Electrodynamics brand.
Look for Siemens model number 10185464 and serial numbers 1308-1311, 1313 on the coil's label.
Reach out to Quality Electrodynamics for return instructions if you have the affected model and serial numbers.
The affected coils have Siemens model number 10185464.
Serial numbers 1308, 1309, 1310, 1311, and 1313 are affected.
The recall does not specify immediate stop-use; contact Quality Electrodynamics for instructions.
We’ve drafted a message you can send Quality Electrodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0033-2020 — Quality Electrodynamics Quality Electrodynamics Hello, I own a Quality Electrodynamics that is covered by recall Z-0033-2020 from Quality Electrodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
